Yôko Shôji

1.9k total citations
63 papers, 1.5k citations indexed

About

Yôko Shôji is a scholar working on Molecular Biology, Epidemiology and Biotechnology. According to data from OpenAlex, Yôko Shôji has authored 63 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 18 papers in Epidemiology and 16 papers in Biotechnology. Recurrent topics in Yôko Shôji's work include Transgenic Plants and Applications (15 papers), RNA Interference and Gene Delivery (11 papers) and Influenza Virus Research Studies (8 papers). Yôko Shôji is often cited by papers focused on Transgenic Plants and Applications (15 papers), RNA Interference and Gene Delivery (11 papers) and Influenza Virus Research Studies (8 papers). Yôko Shôji collaborates with scholars based in Japan, United States and Germany. Yôko Shôji's co-authors include Hideki Nakashima, Vidadi Yusibov, Jessica A. Chichester, Konstantin Musiychuk, Hong Bi, Vadim Mett, Ammasi Periasamy, Saghir Akhtar, Brian Herman and R. L. Juliano and has published in prestigious journals such as Nucleic Acids Research, Journal of Controlled Release and Experimental Cell Research.

In The Last Decade

Yôko Shôji

61 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Yôko Shôji Japan 21 797 466 264 261 205 63 1.5k
Nobuyuki Matoba United States 25 1.2k 1.5× 677 1.5× 191 0.7× 130 0.5× 329 1.6× 65 1.8k
Kristiina Takkinen Finland 23 820 1.0× 257 0.6× 249 0.9× 97 0.4× 126 0.6× 46 1.6k
Jesse M. Jaynes United States 25 1.0k 1.3× 311 0.7× 95 0.4× 140 0.5× 259 1.3× 81 1.8k
Kee‐Jong Hong South Korea 18 537 0.7× 172 0.4× 193 0.7× 165 0.6× 218 1.1× 55 1.4k
Sylvia A. McPherson United States 24 1.2k 1.5× 200 0.4× 341 1.3× 191 0.7× 291 1.4× 39 2.0k
Pierre L. Goossens France 29 1.1k 1.4× 587 1.3× 335 1.3× 249 1.0× 416 2.0× 61 2.1k
Nicolas Tarbouriech France 25 613 0.8× 200 0.4× 319 1.2× 671 2.6× 132 0.6× 43 1.7k
Irma van Die Netherlands 29 1.1k 1.4× 197 0.4× 278 1.1× 265 1.0× 1.2k 6.0× 52 2.7k
R. Assenberg United Kingdom 18 1.0k 1.3× 117 0.3× 278 1.1× 191 0.7× 145 0.7× 23 1.7k
Aaron T. Whiteley United States 19 1.1k 1.4× 307 0.7× 311 1.2× 233 0.9× 649 3.2× 26 1.9k

Countries citing papers authored by Yôko Shôji

Since Specialization
Citations

This map shows the geographic impact of Yôko Shôji's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yôko Shôji with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yôko Shôji more than expected).

Fields of papers citing papers by Yôko Shôji

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yôko Shôji. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yôko Shôji. The network helps show where Yôko Shôji may publish in the future.

Co-authorship network of co-authors of Yôko Shôji

This figure shows the co-authorship network connecting the top 25 collaborators of Yôko Shôji. A scholar is included among the top collaborators of Yôko Shôji based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yôko Shôji. Yôko Shôji is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Musiychuk, Konstantin, Yôko Shôji, Stephen Tottey, et al.. (2024). Basic leucine zipper transcription activators – tools to improve production and quality of human erythropoietin in Nicotiana benthamiana. Biotechnology Journal. 19(5). e2300715–e2300715. 1 indexed citations
2.
3.
Chichester, Jessica A., Brian J. Green, R. Mark Jones, et al.. (2018). Safety and immunogenicity of a plant-produced Pfs25 virus-like particle as a transmission blocking vaccine against malaria: A Phase 1 dose-escalation study in healthy adults. Vaccine. 36(39). 5865–5871. 90 indexed citations
4.
Shôji, Yôko, Jessica A. Chichester, Gene A. Palmer, et al.. (2011). An influenza N1 neuraminidase-specific monoclonal antibody with broad neuraminidase inhibition activity against H5N1 HPAI viruses. Human Vaccines. 7(sup1). 199–204. 20 indexed citations
5.
Asai, Daisuke, Akira Tsuchiya, Jeong‐Hun Kang, et al.. (2009). Inflammatory cell‐specific transgene expression system responding to Iκ‐B kinase beta activation. The Journal of Gene Medicine. 11(7). 624–632. 16 indexed citations
6.
Asai, Daisuke, Yôko Shôji, Jeong‐Hun Kang, et al.. (2009). Specific transgene expression in HIV-infected cells using protease-cleavable transcription regulator. Journal of Controlled Release. 141(1). 52–61. 13 indexed citations
7.
Shôji, Yôko, Hong Bi, Konstantin Musiychuk, et al.. (2008). Plant-derived hemagglutinin protects ferrets against challenge infection with the A/Indonesia/05/05 strain of avian influenza. Vaccine. 27(7). 1087–1092. 86 indexed citations
8.
Shôji, Yôko, Jessica A. Chichester, Hong Bi, et al.. (2008). Plant-expressed HA as a seasonal influenza vaccine candidate. Vaccine. 26(23). 2930–2934. 80 indexed citations
9.
Takayama‐Ito, Mutsuyo, Ken‐ichi Inoue, Yôko Shôji, et al.. (2006). A highly attenuated rabies virus HEP-Flury strain reverts to virulent by single amino acid substitution to arginine at position 333 in glycoprotein. Virus Research. 119(2). 208–215. 61 indexed citations
10.
Kodama, Kota, Yôko Shôji, Hideki Nakashima, et al.. (2005). Artificial Gene Regulation System Responding to HIV Protease. 2004. 675–676.
11.
Shôji, Yôko, et al.. (1998). Enhancement of Anti-Herpetic Activity of Antisense Phosphorothioate Oligonucleotides 5′ End Modified with Geraniol. Journal of drug targeting. 5(4). 261–273. 9 indexed citations
12.
Shôji, Yôko, et al.. (1998). Limited Use of Cationic Liposomes as Tools to Enhance the Antiherpetic Activities of Oligonucleotides in Vero Cells Infected with Herpes Simplex Virus Type 1. Antisense and Nucleic Acid Drug Development. 8(4). 255–263. 5 indexed citations
13.
Shôji, Yôko. (1996). Basic examination of effects of antisense oligonucleotide for rabbit herpes keratitis.. Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics. 27(1). 309–310. 1 indexed citations
14.
Shôji, Yôko, Jingoro Shimada, & Yutaka Mizushima. (1995). The factors to reflect on the subcellular distribution of antisense DNA.. Drug Delivery System. 10(2). 85–90. 2 indexed citations
15.
Shôji, Yôko, et al.. (1994). Characteristic of cellular uptake mechanism and subcellular distribution of phosphorothioate oligodeoxynucleotides in CHRC5 cells.. Drug Delivery System. 9(1). 19–24. 1 indexed citations
16.
Higaki, Megumu, et al.. (1993). Effects of IL-1.BETA. expression in synobiocytes from patients with RA by antisense DNA.. Drug Delivery System. 8(4). 257–261. 1 indexed citations
17.
Hayakawa, Eiji, Akira Yamamoto, Yôko Shôji, & Vincent H.L. Lee. (1989). Effect of sodium glycocholate and polyoxyethylene-9-lauryl ether on the hydrolysis of varying concentrations of insulin in the nasal homogenates of the albino rabbit. Life Sciences. 45(2). 167–174. 20 indexed citations
18.
Shôji, Yôko, Yutaka Mizushima, & Tetsuji Kametani. (1986). The Interaction of Lipid Microspheres and MM46 Tumor Cells. YAKUGAKU ZASSHI. 106(7). 605–608. 7 indexed citations
19.
Yanagawa, Akira, et al.. (1983). Immuno-modulating effects of CCA in C3H/He mice. Ensho. 3(2). 156–157. 1 indexed citations
20.
Hiramoto, Yukio & Yôko Shôji. (1982). Location of the motive force for chromosome movement in sand dollar eggs. Cell Differentiation. 11(5-6). 349–351. 10 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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